Hand position during chest compressions: interlocked fingers vs. overlapped hands

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In a randomized crossover simulation, healthy adult participants perform two 2-minute chest compression periods using interlocked fingers and overlapped hands, in random order, with a 10-minute rest between sessions. The primary outcome is average compression depth, while secondary outcomes include compression rate, proportion of adequate depth and full recoil, depth changes over time, and subjective measures of pain, fatigue, hand stability, and confidence. The study uses an adult CPR manikin in a simulated environment at the University of Pécs, with each participant serving as their own control. Findings will inform whether the non-interlocked hand position is a viable alternative to the interlocked-finger technique for CPR quality and rescuer comfort.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adults aged 18 years or older
* Healthcare professionals or laypersons
* Physically able to perform chest compressions
* Able and willing to provide written informed consent to participate in the study

Exclusion Criteria:

* Acute injury of the upper extremities
* Chronic musculoskeletal disease or symptoms that may interfere with the ability to perform chest compressions with adequate quality
* technical issue during data collection

Where it's running

• University of Pécs
  Pécs, Hungary Recruiting

Study contacts

• Principal investigator: Bálint Bánfai, PhD — University of Pécs Faculty of Health Sciences
• Study coordinator: Bálint Bánfai, PhD
• Email: balint.banfai@etk.pte.hu
• Phone: +3672501-500

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Smartphone-based EEG to detect hidden awareness in ICU patients with brain injuries

  Researchers will test a smartphone-enabled EEG to see if it can reveal Cognitive Motor Dissociation in ICU patients who can’t show commands at bedside.

  Recruiting Columbia University · Miami, Florida and 8 other locations · NCT07917728

• Physiology-guided Epinephrine Dosing in Pediatric Cardiac Arrest

  This observational study looks at how a child’s body responds to epinephrine during in-hospital cardiac arrests to see if dosing can be guided by physiology.

  Recruiting at 22 sites Children's Hospital of Philadelphia · Orange, California and 21 other locations · NCT07890610

• Risk of malignant arrhythmias after acute coronary syndrome

  This study tracks how often dangerous heart rhythms occur in adults admitted for ACS and looks for patterns that might predict them.

  Recruiting Catharina Ziekenhuis Eindhoven · Eindhoven, North Brabant · NCT07824050

• Hyperacute Neurobiomarker Kinetics in Acute Brain Injury: What Happens in Minutes After Injury

  This study tests how early brain injury biomarkers behave in the first minutes to hours after traumatic brain injury or cardiac arrest to see if they rise quickly enough to help with early care.

  Recruiting at 4 sites University of Pecs · Pécs, Branya and 3 other locations · NCT07782216

• Augmented reality CPR feedback for pediatric resuscitation

  This study tests whether AR-CPR feedback can help healthcare teams deliver high-quality chest compressions in simulated pediatric cardiac arrest, as compared with coaching from a CPR expert.

  Recruiting at 8 sites Johns Hopkins University · St. Petersburg, Florida and 7 other locations · NCT07778823

• Adapted CPR Strategy for Adults in Cardiac Arrest

  This trial tests whether a modified advanced life support algorithm improves return of spontaneous circulation in adults who suffer a cardiac arrest before reaching the hospital.

  Recruiting Johannes Kepler University of Linz · Linz, Upper Austria · NCT07754656

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.